Site Staff Training

Whatever your background is - whether you already have experience in Clinical Research, or are new to the field, - we have the course for you! Our monthly courses, approved by Ethic Committees, Sponsors and the German Medical Association (Bundesaerztekammer), focus on recent developments in Clinical Research, the latest legal and regulatory guidelines, and equip you with the necessary knowledge and skills to ensure that you feel competent and at ease conducting clinical trials. 

Prüfarzt und Study Nurse

Site Staff Training

GCP for Investigators

To ensure the safety and well-being of subjects and patients at all times, clinical trials need to be carried out to the highest quality standards and in accordance with national and international guidelines. This seminar equips prospective Clinical Investigators with the necessary skills and knowledge for conducting clinical trials, based on a sound understanding of Good Clinical Practice (GCP), the legal framework, ethical considerations, and the roles and responsibilities of all parties involved in a trial.

Study Nurse Training

This 5-day intensive program teaches the basic principles of clinical research, and gives a thorough insight into how clinical trials are conducted in hospitals and doctors’ practices. It focuses particularly on the recent developments in the field of clinical research and the latest legal and regulatory guidelines (ICH-GCP/AMG).

GCP Refresher for Investigators

Kompaktkurs für erfahrene Prüfer, Stellvertreter und ärztliche Mitglieder einer Prüfgruppe bei klinischen Prüfungen nach Arzneimittelgesetz AMG

(ENGLISCHE ÜBERSETZUNG FEHLT)

GCP REFRESHER FOR STUDY NURSES

Professional and well-trained study teams are necessary to ensure that clinical trials are carried out in accordance with national and international guidelines. As the primary contact for patients, Investigators and Clinical Monitors Study Nurses ensure that everything runs smoothly at the site, look after subjects, collect and record relevant study data and prepare for monitoring visits and audits. This practical course brings your knowledge and skills up-to-date, and enables you to work independently and play a more responsible role in the conduct of clinical trials.